Measuring G protein-coupled receptor signalling in the brain with resonance energy transfer based biosensors

被引:3
作者
Jones-Tabah, Jace [1 ]
Clarke, Paul B. S. [1 ]
Hebert, Terence E. [1 ]
机构
[1] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
MU-OPIOID RECEPTOR; DOPAMINE D2 RECEPTOR; IN-VIVO; BIASED AGONISM; FUNCTIONAL SELECTIVITY; FLUORESCENT PROTEINS; CELLULAR-RESOLUTION; NEURONAL-ACTIVITY; CIRCUIT DYNAMICS; CRE-RECOMBINASE;
D O I
10.1016/j.coph.2016.10.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Activation of a G protein-coupled receptor (GPCR) triggers downstream signalling pathways whose identity is determined not only by the genetic background of the cell, but also by the interacting ligand. Assays that measure endogenous GPCR signalling in vivo are needed to specify the intracellular signalling pathways leading to therapeutic vs. adverse outcomes in animal models. To this end, genetically encoded biosensors can be expressed in vivo with cell type specificity to report GPCR signalling in real time. Biosensor imaging is facilitated by novel microscopic and photometric techniques developed for imaging in behaving animals. The techniques discussed here herald a new wave of in vivo signalling studies that will help identify therapeutically relevant signalling, and design functionally selective drugs for neuropsychiatric diseases.
引用
收藏
页码:44 / 48
页数:5
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